Optimizing PGRs for in vitro shoot proliferation of pomegranate with bayesian-tuned ensemble stacking regression and NSGA-II: a comparative evaluation of machine learning models.

IF 4.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Saeedeh Zarbakhsh, Ali Reza Shahsavar, Mohammad Soltani
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引用次数: 0

Abstract

Background: The process of optimizing in vitro shoot proliferation is a complicated task, as it is influenced by interactions of many factors as well as genotype. This study investigated the role of various concentrations of plant growth regulators (zeatin and gibberellic acid) in the successful in vitro shoot proliferation of three Punica granatum cultivars ('Faroogh', 'Atabaki' and 'Shirineshahvar'). Also, the utility of five Machine Learning (ML) algorithms-Support Vector Regression (SVR), Random Forest (RF), Extreme Gradient Boosting (XGB), Ensemble Stacking Regression (ESR) and Elastic Net Multivariate Linear Regression (ENMLR)-as modeling tools were evaluated on in vitro multiplication of pomegranate. A new automatic hyperparameter optimization method named Adaptive Tree Pazen Estimator (ATPE) was developed to tune the hyperparameters. The performance of the models was evaluated and compared using statistical indicators (MAE, RMSE, RRMSE, MAPE, R and R2), while a specific Global Performance Indicator (GPI) was introduced to rank the models based on a single parameter. Moreover, Non‑dominated Sorting Genetic Algorithm‑II (NSGA‑II) was employed to optimize the selected prediction model.

Results: The results demonstrated that the ESR algorithm exhibited higher predictive accuracy in comparison to other ML algorithms. The ESR model was subsequently introduced for optimization by NSGA‑II. ESR-NSGA‑II revealed that the highest proliferation rate (3.47, 3.84, and 3.22), shoot length (2.74, 3.32, and 1.86 cm), leave number (18.18, 19.76, and 18.77), and explant survival (84.21%, 85.49%, and 56.39%) could be achieved with a medium containing 0.750, 0.654, and 0.705 mg/L zeatin, and 0.50, 0.329, and 0.347 mg/L gibberellic acid in the 'Atabaki', 'Faroogh', and 'Shirineshahvar' cultivars, respectively.

Conclusions: This study demonstrates that the 'Shirineshahvar' cultivar exhibited lower shoot proliferation success compared to the other cultivars. The results indicated the good performance of ESR-NSGA-II in modeling and optimizing in vitro propagation. ESR-NSGA-II can be applied as an up-to-date and reliable computational tool for future studies in plant in vitro culture.

利用贝叶斯调整的集合堆叠回归和 NSGA-II 优化石榴离体芽增殖的 PGRs:机器学习模型的比较评估。
背景:优化离体芽增殖的过程是一项复杂的任务,因为它受到许多因素和基因型相互作用的影响。本研究调查了不同浓度的植物生长调节剂(玉米素和赤霉素)在三个石榴栽培品种('Faroogh'、'Atabaki'和'Shirineshahvar')体外芽增殖成功中的作用。此外,还评估了五种机器学习(ML)算法--支持向量回归(SVR)、随机森林(RF)、极端梯度提升(XGB)、集合堆积回归(ESR)和弹性网多元线性回归(ENMLR)--作为建模工具在石榴离体增殖中的实用性。开发了一种新的自动超参数优化方法,名为自适应树帕森估计器(ATPE),用于调整超参数。利用统计指标(MAE、RMSE、RRMSE、MAPE、R 和 R2)对模型的性能进行了评估和比较,同时引入了一个特定的全局性能指标(GPI),根据单一参数对模型进行排序。此外,还采用了非优势排序遗传算法-II(NSGA-II)来优化选定的预测模型:结果表明,与其他 ML 算法相比,ESR 算法的预测准确率更高。随后,ESR 模型被引入 NSGA-II 进行优化。ESR-NSGA-II 发现,ESR-NSGA-II 的增殖率(3.47、3.84 和 3.22)、芽长(2.74、3.32 和 1.86 厘米)、叶片数(18.18、19.76 和 18.77)和外植体存活率(84.21%、85.49% 和 56.39%)最高。结论:这项研究表明,"Shirineshahvar"、"Atabaki "和 "Faroogh "在含有 0.750、0.654 和 0.705 毫克/升玉米素以及 0.50、0.329 和 0.347 毫克/升赤霉素的培养基中,均能获得较高的生长效率:本研究表明,与其他栽培品种相比,'Shirineshahvar'栽培品种的芽增殖成功率较低。结果表明,ESR-NSGA-II 在体外繁殖建模和优化方面具有良好的性能。ESR-NSGA-II 可作为一种最新、可靠的计算工具,用于今后的植物离体培养研究。
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来源期刊
Plant Methods
Plant Methods 生物-植物科学
CiteScore
9.20
自引率
3.90%
发文量
121
审稿时长
2 months
期刊介绍: Plant Methods is an open access, peer-reviewed, online journal for the plant research community that encompasses all aspects of technological innovation in the plant sciences. There is no doubt that we have entered an exciting new era in plant biology. The completion of the Arabidopsis genome sequence, and the rapid progress being made in other plant genomics projects are providing unparalleled opportunities for progress in all areas of plant science. Nevertheless, enormous challenges lie ahead if we are to understand the function of every gene in the genome, and how the individual parts work together to make the whole organism. Achieving these goals will require an unprecedented collaborative effort, combining high-throughput, system-wide technologies with more focused approaches that integrate traditional disciplines such as cell biology, biochemistry and molecular genetics. Technological innovation is probably the most important catalyst for progress in any scientific discipline. Plant Methods’ goal is to stimulate the development and adoption of new and improved techniques and research tools and, where appropriate, to promote consistency of methodologies for better integration of data from different laboratories.
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